CAF Specific Expression of Podoplanin May Be Dispensable for the Malignancy of Malignant Melanoma

Within the tumor microenvironment (TME), cancer-associated fibroblasts (CAFs) were shown to be an active and pivotal cell population, supporting many protumorigenic mechanisms. Podoplanin (PDPN)-positive CAFs are of special interest since their abundance correlated with a worse prognosis for patients of different cancer entities, including malignant melanoma. In this study, we applied a loss-of-function approach in an in vivo mouse melanoma model to evaluate the contribution of CAF-specific PDPN expression to melanoma formation and progression. Surprisingly, despite its prominent expression in CAFs deletion of PDPN in this cell type did neither affect the onset, nor growth of MM tumors. These data imply that PDPN expression in CAFs represents a biomarker for poor prognosis but does not serve as a useful target for stroma-directed therapy of malignant melanoma.

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Publication Details

Journal
Molecular Carcinogenesis
Published
2024-11-08
DOI
https://doi.org/10.1002/mc.23841
Citations
3
Primary Topic
Lymphatic System and Diseases
Type
article
Field-Weighted Citation Impact
0.85

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article

CAF Specific Expression of Podoplanin May Be Dispensable for the Malignancy of Malignant Melanoma

Saskia Tauch, Peter Angel, Melanie Sator‐Schmitt, Sabrina Lohr et al.
3 citations
Molecular Carcinogenesis
Lymphatic System and Diseases
0.85
article

CAF Specific Expression of Podoplanin May Be Dispensable for the Malignancy of Malignant Melanoma

Saskia Tauch, Peter Angel, Melanie Sator‐Schmitt, Sabrina Lohr, Hellmut G. Augustin, Bettina Kast, Nicolas Gengenbacher, Lowis Kemm
article en
3 citations

Abstract

Within the tumor microenvironment (TME), cancer-associated fibroblasts (CAFs) were shown to be an active and pivotal cell population, supporting many protumorigenic mechanisms. Podoplanin (PDPN)-positive CAFs are of special interest since their abundance correlated with a worse prognosis for patients of different cancer entities, including malignant melanoma. In this study, we applied a loss-of-function approach in an in vivo mouse melanoma model to evaluate the contribution of CAF-specific PDPN expression to melanoma formation and progression. Surprisingly, despite its prominent expression in CAFs deletion of PDPN in this cell type did neither affect the onset, nor growth of MM tumors. These data imply that PDPN expression in CAFs represents a biomarker for poor prognosis but does not serve as a useful target for stroma-directed therapy of malignant melanoma.

Molecular CarcinogenesisVol. 64(2)
German Cancer Research Center (DE), Heidelberg University (DE), University Hospital Heidelberg (DE), DKFZ-ZMBH Alliance (DE), University Medical Centre Mannheim (DE)
Deutsches Krebsforschungszentrum
No poverty
Openalex Percentile: Top 22%
Lymphatic System and Diseases
0.85
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